Maximum Turnover Number Research Articles

Base-free aqueous Suzuki–Miyaura coupling reaction using recoverable bi-functional Pd supported nanocatalyst

A solid base catalyst comprising pyridine-palladium polyorganosiloxane framework was synthesized via a grafting method. The resulting organic–inorganic hybrid palladium nanomaterial was characterized by 13C CP-MAS NMR, 29Si CP-MAS NMR, XRD, EDX, TEM, TGA, and the BET measurements. The hybrid palladium nanomaterial exhibited high catalytic activity for the Suzuki–Miyaura cross-coupling reaction between aryl chlorides and phenylboronic acid under base-free and aerobic conditions. A maximum turnover number (TON) of 3150, with a 0.2 mol% Pd loading and a reaction temperature of 80 °C in aqueous solution. The catalyst demonstrated remarkable stability, maintaining its activity even after six cycles of reuse without significant loss of activity. TEM images showed that the catalyst retained its structure and high-order mesostructure after several uses. ICP-AES also confirmed the absence of palladium contamination in the final products. Leaching test studies further confirmed the true heterogeneous nature of the developed catalytic system.

Electronic Effects in Cobalt Phthalocyanine Catalysts Towards Noble-Metal-Free, Photocatalytic CO2-to-CO Reduction.

Noble-metal-free CO2 reduction systems based on cobalt phthalocyanine (CoPc) and its derivatives have demonstrated remarkable photocatalytic performances; however, their structure-activity relationship with electronic tuning remains unexplored. Herein, we now provide a systematic study to investigate the electron effects of substituents on the CoPc family in photocatalytic CO2 reduction, where a Cu(I) heteroleptic photosensitizer is utilized. The highest performance can be achieved using cobalt tetracarboxylphthalocyanine in light-driven CO2-to-CO reduction, with a maximum turnover number of 2950 at 450 nm and an outstanding apparent quantum yield of 63.5% at 425 nm, over ten times the activity with the tetra-dimethylamino-substituted CoPc derivative. The favorable electron-withdrawing effects have been further verified by DFT calculations and cyclic voltammetry, which reduces the overpotential required for CO2 reduction and decreases the Gibbs free energy of the catalyst active intermediates, particularly the CO-desorption energetics.

Revisiting the catalytic activity of single horseradish peroxidase clusters through electrochemical collision technique: Effect of electrolyte and substrate

Horseradish peroxidase (HRP) is a versatile biosensing label and signal reporter owing to its broad-spectrum catalytic ability. In present work, we characterized HRP's catalytic performance with various substrates using electrochemical collision technique and analyzed the associated electron transfer processes. Different electrolyte solutions greatly affected enzyme dispersibility and zeta potential, thereby impacting HRP collision dynamics in single H2O2 substrate system. The maximum turnover number (kcat) for single HRP molecules was calculated to be 3.611 ± 0.149 × 103 s−1 in 0.85 % NaCl and 2.967 ± 0.286 × 103 s−1 in 0.1 M PBS solution, reflecting differences in cluster size induced by the electrolyte conditions. More severe agglomeration of HRP molecules was observed in double-substrate systems, where the hydrophilic mediator (K4Fe(CN)6) and lipophilic mediator (ABTS) served as electron donors and signal reporters. The calculated kcat value of single HRP molecules in ABTS-H2O2 was 7.6 times higher than that in K4Fe(CN)6–H2O2. This difference is attributed to mediators' solubility, lipophilicity, and HRP's affinity for different substrates, with HRP demonstrated stronger affinity for ABTS-H2O2 substrates, which realized more efficient electron transfer and compensated for the low diffusion coefficient of ABTS. This work provides a comprehensive analysis of the effects of electrolytes and substrates on HRP collision and catalytic behavior, offering valuable insights for the advanced design of HRP-based biosensors and diagnostic platforms.

Strong Enhancement in Cobalt(II)‐TPMA Aqueous Hydrogen Photosynthesis through Intramolecular Proton Relay

AbstractPhotosynthetic hydrogen generation by cobalt(II) tris(2‐pyridylmethyl)amine (TPMA) complexes is mainly limited by protonation kinetics and decomposition routes involving demetallation. In the present work we have explored the effects of both proton shuttles and improved rigidity on the catalytic ability of cobalt(II) TPMA complexes. Remarkably, we demonstrate that, while a small enhancement in the catalytic performance is attained in a rigid cage structure, the introduction of ammonium groups as proton transfer relays in close proximity to the cobalt center allows to reach a 4‐fold increase in the quantum efficiency of H2 formation, and a surprising 22‐fold gain in the maximum turnover number, at low catalyst concentration. The beneficial role of the ammonium relays in promoting faster intramolecular proton transfer to the reduced cobalt center is documented by transient absorption spectroscopy, showcasing the great relevance of tuning the catalyst periphery to achieve efficient catalysis of solar fuel formation.

MaxKinEff: A Collision Theory-Based Approach for Analyzing Turnover Frequency and Turnover Number in Catalytic Processes.

The efficiency of catalysts relies on comprehending the underlying kinetics that govern their performance. Under the steady-state regime, the "rate" is referred to as the turnover frequency, where the reaction rate is first order with respect to catalysts. Here, we introduce the Maximum Kinetic Efficiency (MaxKinEff) model, grounded in collision theory, to predict efficiency based on maximum turnover frequency, and maximum turnover number, . The model was applied to molecular water oxidation using twenty-six transition metal catalysts from the first (3d), second (4d), and third (5d) rows. A thorough investigation reveals that [Ru(pda)(Br-py)2] (pda=1,10-phenanthroline-2,9-dicarboxylate; Py=pyridinophane) exhibits a notable of 1176.87×10-5 s-1 due to its larger collision diameter (σRC) and lower activation energy (Ea). Importantly, the trend in the computed values aligns with experimental TON, validating the model's accuracy. For instance, [Cp*Ir(κ2-N,O)NO3] is identified by MaxKinEff as a standout performer, with the normalized maximum computed TON, resembling the experimental TON, =2000.

Unveiling the Reactivity of Part Per Million Levels of Cobalt-Salen Complexes in Hydrosilylation of Ketones.

A series of air-stable cobalt(III)salen complexes Co-1 to Co-4 have been synthesized and employed in the hydrosilylation of ketones. Notably, the most intricately tailored Co-3 pre-catalyst exhibited exceptional catalytic activity under mild reaction conditions. The developed catalytic hydrosilylation protocol proceeded with an unusual ppm level (5 ppm) catalyst loading of Co-3 and achieved a maximum turnover number (TON) of 200,000. A wide variety of aromatic, aliphatic, and heterocyclic ketones encompassing both electron-donating and electron-withdrawing substituents were successfully transformed into the desired silyl ethers or secondary alcohols in moderate to excellent yields.

Strong Enhancement in Cobalt(II)-TPMA Aqueous Hydrogen Photosynthesis through Intramolecular Proton Relay.

Photosynthetic hydrogen generation by cobalt(II) tris(2-pyridylmethyl)amine (TPMA) complexes is mainly limited by protonation kinetics and decomposition routes involving demetallation. In the present work we have explored the effects of both proton shuttles and improved rigidity on the catalytic ability of cobalt(II) TPMA complexes. Remarkably, we demonstrate that, while a small enhancement in the catalytic performance is attained in a rigid cage structure, the introduction of ammonium groups as proton transfer relays in close proximity to the cobalt center allows to reach a 4-fold increase in the quantum efficiency of H2 formation, and a surprising 22-fold gain in the maximum turnover number, at low catalyst concentration. The beneficial role of the ammonium relays in promoting faster intramolecular proton transfer to the reduced cobalt center is documented by transient absorption spectroscopy, showcasing the great relevance of tuning the catalyst periphery to achieve efficient catalysis of solar fuel formation.

Metal-acid synergistic catalysis accelerates the hydrogen borrowing amination of alcohols by confining Ru sites in Beta zeolite

Direct hydrogen transfer amination of alcohols with amines is an environmentally friendly and atom-economical route for the synthesis of N-alkylamines. Noble metal species are highly catalytic active sites, but the exorbitant price makes the urgency to boost the atom efficiency with stable recyclability. Herein, we demonstrated that encapsulation of Ru nanoparticles (NPs) within BEA zeolite through direct hydrothermal approach greatly promoted the catalytic efficiency in the N-alkylation of aromatic alcohols and amines under additive- and solvent-free conditions, resulting in the high yield (∼93 %), maximum turnover number (TON) of 12,822 and turnover frequency (TOF) of 9012 h−1, with stable recyclability and extendable substrate scope. The kinetic studies and in-situ characterizations revealed that the synergy of confined Ru NPs and adjacent acid sites of BEA zeolite significantly promoted the C–H bond activation in the rate-determining step of alcohol dehydrogenation into aldehydes. Besides, the acid sites also accelerated the condensation of aldehyde intermediates and anilines to promote the kinetic equilibrium, while the moderate strength of the Ru–H bond resulting from the confined Ru NPs is advantageous to balance the dehydrogenation and hydrogenation steps to reach the fascinating H-transfer process.

Turnover Number in Photoinduced Molecular Catalysis of Hydrogen Evolution: a Benchmarking for Catalysts?

Development of devices for production of H2 using light and a sustainable source of electrons may require the design of molecular systems combining a molecular catalyst and a photosensitizer. Evaluation of the efficiency of hydrogen production is commonly performed in homogeneous solution with a sacrificial electron donor and the report of the maximal turnover number vs catalyst ( ). This figure of merit is strongly dependent on deactivation pathways and does not by itself provide a benchmarking for catalysts. In particular, when the photosensitizer degradation is the primary source of limitation, a kinetic model, rationalizing literature data, shows that a decrease of the catalyst concentration leads to an increase of . It indicates that exceptionally high obtained at very low catalyst concentration shall not be considered as an indication of an exceptional catalytic system. We advocate for a systematic kinetic analysis in order to get a quantitative measure of the competitive pathways leading to values and to provide keys for performance improvement.

Designing Degradable Polymers from Tricycloalkenes via Complete Cascade Metathesis Polymerization.

Cascade metathesis polymerization has been developed as a promising method to synthesize complex but well-defined polymers from monomers containing multiple reactive functional groups. However, this approach has been limited to the monomers involving simple alkene/alkyne moieties or produced mainly non-degradable polymers. In this study, we demonstrate a complete cascade ring-opening/ring-closing metathesis polymerization (RORCMP) using various tricycloalkenes and two strategies for the efficient degradation. Through rational design of tricycloalkene monomers, the structure and reactivity relationship was explored. For example, tricycloalkenes with trans configuration in the central ring enabled faster and better selective cascade RORCMP than the corresponding cis isomers. Also, a 4-substituted cyclopentene moiety in the monomers significantly enhanced the overall cascade RORCMP performance, with the maximum turnover number (TON) reaching almost 10,000 and molecular weight up to 170 kg/mol using an amide-containing monomer. Furthermore, we achieved one-shot cascade multiple olefin metathesis polymerization using tricycloalkenes and a diacrylate, to produce new highly A,B-alternating copolymers with full degradability. Lastly, we successfully designed xylose-based tricycloalkenes to give well-defined polymers that underwent ultra-fast and complete degradation under mild conditions.

Designing Degradable Polymers from Tricycloalkenes via Complete Cascade Metathesis Polymerization

AbstractCascade metathesis polymerization has been developed as a promising method to synthesize complex but well‐defined polymers from monomers containing multiple reactive functional groups. However, this approach has been limited to the monomers involving simple alkene/alkyne moieties or produced mainly non‐degradable polymers. In this study, we demonstrate a complete cascade ring‐opening/ring‐closing metathesis polymerization (RORCMP) using various tricycloalkenes and two strategies for the efficient degradation. Through rational design of tricycloalkene monomers, the structure and reactivity relationship was explored. For example, tricycloalkenes with trans configuration in the central ring enabled faster and better selective cascade RORCMP than the corresponding cis isomers. Also, a 4‐substituted cyclopentene moiety in the monomers significantly enhanced the overall cascade RORCMP performance, with the maximum turnover number (TON) reaching almost 10,000 and molecular weight up to 170 kg/mol using an amide‐containing monomer. Furthermore, we achieved one‐shot cascade multiple olefin metathesis polymerization using tricycloalkenes and a diacrylate, to produce new highly A,B‐alternating copolymers with full degradability. Lastly, we successfully designed xylose‐based tricycloalkenes to give well‐defined polymers that underwent ultra‐fast and complete degradation under mild conditions.

Unveiling the Broad Substrate Specificity of Deoxynivalenol Oxidation Enzyme DepA and Its Role in Detoxifying Trichothecene Mycotoxins.

DepA, a pyrroloquinoline quinone (PQQ)-dependent enzyme isolated from Devosia mutans 17-2-E-8, exhibits versatility in oxidizing deoxynivalenol (DON) and its derivatives. This study explored DepA's substrate specificity and enzyme kinetics, focusing on DON and 15-acetyl-DON. Besides efficiently oxidizing DON, DepA also transforms 15-acetyl-DON into 15-acetyl-3-keto-DON, as identified via LC-MS/MS and NMR analysis. The kinetic parameters, including the maximum reaction rate, turnover number, and catalytic efficiency, were thoroughly evaluated. DepA-PQQ complex docking was deployed to rationalize the substrate specificity of DepA. This study further delves into the reduced toxicity of the transformation products, as demonstrated via enzyme homology modeling and in silico docking analysis with yeast 80S ribosomes, indicating a potential decrease in toxicity due to lower binding affinity. Utilizing the response surface methodology and central composite rotational design, mathematical models were developed to elucidate the relationship between the enzyme and cofactor concentrations, guiding the future development of detoxification systems for liquid feeds and grain processing. This comprehensive analysis underscores DepA's potential for use in mycotoxin detoxification, offering insights for future applications.

Pt(II)-bis(quinolinyl) complexes for photocatalytic hydrogen production.

Three Pt(II)-bis(quinolinyl) complexes with varying electron densities were synthesized, structurally characterized and used for photocatalytic hydrogen production under different conditions. All the complexes were found to be active for hydrogen production giving a maximum turnover number (TON) of 1230 surpassing the conventionally used Pt-terpyridyl complexes.

Sustainable Immobilization of β-Glucosidase onto Silver Ions and AgNPs-Loaded Acrylic Fabric with Enhanced Stability and Reusability.

Modified polymer design has attracted significant attention for enzyme immobilization, offering promising applications. In this study, amine-terminated polymers were synthesized by incorporating functional groups into polyacrylonitrile using hexamethylenediamine. This work highlights the successful enzyme immobilization strategy using modified polymers, offering improved stability and expanded operational conditions for potential biotechnological applications. The resulting amino groups were utilized to capture silver ions, which were subsequently converted to silver nanoparticles (AgNPs). The obtained materials, AgNPs@TA-HMDA (acrylic textiles coated silver nanoparticles AgNPs) and Ag(I)@TA-HMDA (acrylic textiles coated with Ag ion) were employed as supports for β-glucosidase enzyme immobilization. The highest immobilization yields (IY%) were achieved with AgNPs@TA-HMDA at 92%, followed by Ag(I)@TA-HMDA at 79.8%, resulting in activity yields (AY%) of 81% and 73%, respectively. Characterization techniques such as FTIR, FE-SEM, EDX, TG/DTG, DSC, and zeta potential were employed to investigate the structural composition, surface morphologies, elemental composition, thermal properties, and surface charge of the support materials. After 15 reuses, the preservation percentages decreased to 76% for AgNPs@TA-HMDA/β-Glu and 65% for Ag(I)@TA-HMDA/β-Glu. Storage stability revealed that the decrease in activity for the immobilized enzymes was smaller than the free enzyme. The optimal pH for the immobilized enzymes was broader (pH 5.5 to 6.5) compared to the free enzyme (pH 5.0), and the optimal temperature for the immobilized enzymes was 60 °C, slightly higher than the free enzyme's optimal temperature of 50 °C. The kinetic analysis showed a slight increase in Michaelis constant (Km) values for the immobilized enzymes and a decrease in maximum velocity (Vmax), turnover number (Kcat), and specificity constant (Kcat/Km) values compared to the free enzyme. Through extensive characterization, we gained valuable insights into the structural composition and properties of the modified polymer supports. This research significantly contributes to the development of efficient biotechnological processes by advancing the field of enzyme immobilization and offering valuable knowledge for its potential applications.

Exploring the potential of calcined nanolayered manganese oxides for water-oxidation reaction

Large-scale electrochemical and photochemical hydrogen production methods from water splitting are limited by the water-oxidation reaction (WOR). This study investigates the influence of calcination temperatures on the WOR efficiency of layered Mn oxides, which are known for their stability and high catalytic activity. The Mn oxides were synthesized via thermal decomposition of KMnO4 and characterized using various techniques including scanning electron microscopy, high-resolution transmission electron microscopy, X-ray diffraction, thermal gravimetric analysis, and Raman spectroscopy. The results indicate that even after calcination at high temperatures (≥400 °C), layered Mn oxides remain effective catalysts for WOR. Notably, the calcined sample at 800 °C in cerium (IV) ammonium nitrate at concentrations of 0.30 M shows maximum turnover frequency and turnover number of 6.7 × 10−6/s and 8.6 × 10−3 mol (O2)/mol (Mn) (for 1300 s), respectively.

Modulating the Coordination Environment of Carbon-Dot-Supported Fe Single-Atom Nanozymes for Enhanced Tumor Therapy.

Herein, carbon dot (CD)-supported Fe single-atom nanozymes with high content of pyrrolic N and ultrasmall size (ph-CDs-Fe SAzyme) are fabricated by a phenanthroline-mediated ligand-assisted strategy. Compared with phenanthroline-free nanozymes (CDs-Fe SAzyme), ph-CDs-Fe SAzyme exhibit higher peroxidase (POD)-like activity due to their structure similar to that of ferriporphyrin in natural POD. Aberration-corrected high-angle annular dark field scanning transmission electron microscopy (HAADF-STEM) and X-ray absorption fine structure spectroscopy (XAFS) analyses show that metal Fe is dispersed in ph-CDs-Fe SAzyme as single atoms. Steady-state kinetic studies show that the maximum velocity (Vmax ) and turnover number (kcat ) of H2 O2 homolyticcleavage catalyzed by ph-CDs-Fe SAzyme are 3.0 and 6.2 more than those of the reaction catalyzed by CDs-Fe SAzyme. Density functional theory (DFT) calculations show that the energy barrier of the reaction catalyzed by ph-CDs-Fe SAzyme is lower than that catalyzed by CDs-Fe SAzyme. Antitumor efficacy experiments show that ph-CDs-Fe SAzyme can efficiently inhibit the growth of tumor cells both in vitro and in vivo by synergistic chemodynamic and photothermal effects. Here a new paradigm is provided for the development of efficient antitumor therapeutic approaches based on SAzyme with POD-like activity.

Precious-Metal-Free CO2 Photoreduction Boosted by Dynamic Coordinative Interaction between Pyridine-Tethered Cu(I) Sensitizers and a Co(II) Catalyst.

Improving the photocatalytic efficiency of a fully noble-metal-free system for CO2 reduction remains a fundamental challenge, which can be accomplished by facilitating electron delivery as a consequence of exploiting intermolecular interactions. Herein, we have designed two Cu(I) photosensitizers with different pyridyl pendants at the phenanthroline moiety to enable dynamic coordinative interactions between the sensitizers and a cobalt macrocyclic catalyst. Compared to the parent Cu(I) photosensitizer, one of the pyridine-tethered derivatives boosts the apparent quantum yield up to 76 ± 6% at 425 nm for selective (near 99%) CO2-to-CO conversion. This value is nearly twice that of the parent system with no pyridyl pendants (40 ± 5%) and substantially surpasses the record (57%) of the noble-metal-free systems reported so far. This system also realizes a maximum turnover number of 11 800 ± 1400. In contrast, another Cu(I) photosensitizer, in which the pyridine substituents are directly linked to the phenanthroline moiety, is inactive. The above behavior and photocatalytic mechanism are systematically elucidated by transient fluorescence, transient absorption, transient X-ray absorption spectroscopies, and quantum chemical calculations. This work highlights the advantage of constructing coordinative interactions to fine-tune the electron transfer processes within noble-metal-free systems for CO2 photoreduction.

Light-Driven Hydrogen Evolution Reaction Catalyzed by a Molybdenum-Copper Artificial Hydrogenase.

Orange protein (Orp) is a small bacterial metalloprotein of unknown function that harbors a unique molybdenum/copper (Mo/Cu) heterometallic cluster, [S2MoS2CuS2MoS2]3-. In this paper, the performance of Orp as a catalyst for the photocatalytic reduction of protons into H2 has been investigated under visible light irradiation. We report the complete biochemical and spectroscopic characterization of holo-Orp containing the [S2MoS2CuS2MoS2]3- cluster, with docking and molecular dynamics simulations suggesting a positively charged Arg, Lys-containing pocket as the binding site. Holo-Orp exhibits excellent photocatalytic activity, in the presence of ascorbate as the sacrificial electron donor and [Ru(bpy)3]Cl2 as the photosensitizer, for hydrogen evolution with a maximum turnover number of 890 after 4 h irradiation. Density functional theory (DFT) calculations were used to propose a consistent reaction mechanism in which the terminal sulfur atoms are playing a key role in promoting H2 formation. A series of dinuclear [S2MS2M'S2MS2](4n)- clusters, with M = MoVI, WVI and M'(n+) = CuI, FeI, NiI, CoI, ZnII, CdII were assembled in Orp, leading to different M/M'-Orp versions which are shown to display catalytic activity, with the Mo/Fe-Orp catalyst giving a remarkable turnover number (TON) of 1150 after 2.5 h reaction and an initial turnover frequency (TOF°) of 800 h-1 establishing a record among previously reported artificial hydrogenases.

Enhancing CO2 photoreduction via the perfluorination of Co(II) phthalocyanine catalysts in a noble-metal-free system

The manufacture of high-performance photocatalytic systems based on earth-abundant elements remains a key challenge, urging operative strategies for catalyst design. Herein, we present the construction of an efficient and noble-metal-free molecular system for the photoreduction of CO2 to CO using a Cu(I) photosensitizer and Co(II) phthalocyanine catalysts. It was found that the perfluorination of Co(II) phthalocyanine shows enhanced catalytic performance for CO2-to-CO conversion compared with pristine Co(II) phthalocyanines, achieving a remarkable apparent quantum yield of 58.2% at 425 nm, which is three times that of the pristine one (19.0%). The Cu(I)/Co(II) system also achieved a maximum turnover number of 9185 and near-unity selectivity. These improvements can be attributed to the electron-withdrawing effect of the fluorine substituents, which lowers the catalytic overpotential for catalysis and decreases the Gibbs free energy of the rate-determining Co-carboxylate-forming step. This work indicates that perfluorination is an effective approach to optimize the catalytic performance of molecular catalysts.

Alkoxide-Decorated Copper Nanoparticles on Amidine-Modified Polymers as Hydrogenation Catalysts for Enabling H2 Heterolysis

Direct formation of Cu nanoparticles was accomplished on an amidine- and guanidine-functionalized polymer (polystyrene-bound 1,8-diazabicyclo[5.4.0]undec-7-ene (PS-DBU) and 1,5,7-triazabicyclo[4.4.0]dec-5-ene (PS-TBD), respectively) by thermal treatment of Cu(acac)2 (acac = acetylacetonato) in methanol under pressurized H2. The immobilized structure was characterized by inductively coupled plasma atomic emission spectroscopy (ICP-AES), elemental analysis, and microscopic analysis. X-ray photoelectron spectroscopy (XPS) data indicated that the nanoparticles consisted of Cu(0) and oxygenated Cu(I). The Cu(0)/Cu(I) ratio was determined by X-ray absorption spectroscopy. In particular, X-ray absorption near-edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) studies indicated the inclusion of alkoxides bound to Cu nanoparticles. Further 13C-labeled experiments allowed us to identify the Cu methoxide species by solid-state 13C nuclear magnetic resonance (NMR). A series of alkoxide-incorporated Cu nanoparticles were proven to facilitate H2 heterolysis and were applied in the catalytic hydrogenation of CO2 to formate salts in the presence of a nitrogen base. The catalytic activity increased with decreased mean particle size and increased Cu(I) content, indicating that the Cu(I) alkoxide species played an indispensable role in hydrogenation. The combination of Cu/PS-DBU and 2-tert-butyl-1,1,3,3-tetramethylguanidine (BTMG) achieved a maximum turnover number of 2450 at 100 °C without leaching or aggregation of the nanosized catalysts.